REMODULIN
Remodulin Adverse Events Reported to the FDA Over Time
How are Remodulin adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Remodulin, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Remodulin is flagged as the suspect drug causing the adverse event.
Most Common Remodulin Adverse Events Reported to the FDA
What are the most common Remodulin adverse events reported to the FDA?
| Death | 1839 (34.71%) |
| Dyspnoea | 106 (2%) |
| Diarrhoea | 92 (1.74%) |
| Nausea | 83 (1.57%) |
| Vomiting | 70 (1.32%) |
| Hypotension | 61 (1.15%) |
| Headache | 58 (1.09%) |
| Pneumonia | 50 (.94%) |
| Device Related Infection | 47 (.89%) |
| Sepsis | 47 (.89%) |
| Pain In Extremity | 46 (.87%) |
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This graph shows the top adverse events submitted to the FDA for Remodulin, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Remodulin is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
Adverse Event Categories for Remodulin
What are the most common Remodulin adverse events reported to the FDA?
| Fatal Outcomes | 1845 (34.82%) |
| Infections - Pathogen Unspecified | 413 (7.8%) |
| Respiratory | 193 (3.64%) |
| Gastrointestinal Signs | 191 (3.61%) |
| Bacterial Infectious | 163 (3.08%) |
| Administration Site Reactions | 156 (2.94%) |
| Neurological | 127 (2.4%) |
| Electrolyte And Fluid Balance Condi... | 100 (1.89%) |
| Gastrointestinal Motility And Defec... | 93 (1.76%) |
| Heart Failures | 82 (1.55%) |
| Cardiac Arrhythmias | 81 (1.53%) |
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Share/Embed Graph Export Data
This graph shows the top categories of adverse events submitted to the FDA for Remodulin, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Remodulin is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
Common Uses of Remodulin According to Those Reporting Adverse Events
Why are people taking Remodulin, according to those reporting adverse events to the FDA?
| Pulmonary Arterial Hypertension | 581 |
| Pulmonary Hypertension | 413 |
| Cor Pulmonale Chronic | 137 |
| Product Used For Unknown Indication | 13 |
| Hypertension | 5 |
| Scleroderma | 4 |
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Drug Labels
| Label | Labeler | Effective |
|---|---|---|
| Remodulin | United Therapeutics Corporation | 02-JAN-12 |
Remodulin Case Reports
What Remodulin safety concerns are being reported by doctors and researchers in the medical literature?
About Results
This report contains aggregated drug side effects and adverse events for Remodulin. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.
DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.
DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.
Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.
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